Psychiatry 34 , 10601064 (2010)
Autophagy 19, 20262044
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However, the mainly difference is that the hydrophobic and hydrogen-bonding interactions contributed by the active site residues, H244, E256 and F264 in mushroom tyrosinase are not observed in the corresponding active site residues, P505, S515 and I523 of human tyrosinase (Supplementary Fig
ECs, pericytes, astrocytes, and neurons, among other cell types, collectively modulate cerebral blood flow (CBF) to cater to the high-energy demands of highly active brain regions [2, 3]